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Entry Level Clinical Trials Jobs in Michigan (NOW HIRING)

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Entry Level Clinical Trials information

See Michigan salary details

$25

$54

$83

How much do entry level clinical trials jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for entry level clinical trials in Michigan is $54.49, according to ZipRecruiter salary data. Most workers in this role earn between $44.23 and $61.39 per hour, depending on experience, location, and employer.

What is an entry level clinical trials job?

Entry level clinical trials jobs are positions designed for individuals who are new to the clinical research field and typically have limited or no prior experience. These roles include positions such as Clinical Research Coordinator, Clinical Trial Assistant, or Data Entry Specialist. Responsibilities often involve supporting the planning, implementation, and management of clinical trials, assisting with documentation, handling data, and ensuring compliance with regulatory requirements. Entry level roles usually require a bachelor's degree in a relevant field and strong organizational and communication skills. These positions provide a foundation for career growth within clinical research and drug development.

What are the key skills and qualifications needed to thrive as an entry level clinical trials professional?

To thrive in an entry-level clinical trials role, you need a bachelor's degree in life sciences or a related field, attention to detail, and a solid understanding of clinical research protocols. Familiarity with data management systems, electronic data capture (EDC) tools, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Strong organizational skills, effective communication, and teamwork help you manage study documentation and collaborate with various stakeholders. These skills and qualifications are crucial for ensuring clinical trial compliance, data accuracy, and the smooth execution of research studies.

What are some common challenges faced by entry level clinical trials professionals, and how can they be addressed?

Entry-level professionals in clinical trials often face challenges such as adapting to strict regulatory requirements, managing large volumes of data, and quickly learning specialized medical terminology. It's common to feel overwhelmed at first, but thorough training, mentorship from experienced colleagues, and strong organizational skills can help ease the transition. Open communication within the team and a willingness to ask questions are also key to building confidence and competence in this fast-paced environment.

What is the difference between Entry Level Clinical Trials vs Clinical Research Coordinators?

AspectEntry Level Clinical TrialsClinical Research Coordinators
Required CredentialsHigh school diploma or associate degree; some roles may require certificationBachelor’s degree in health sciences or related field; certification often preferred
Work EnvironmentClinical trial sites, hospitals, research facilitiesResearch sites, hospitals, clinics, pharmaceutical companies
Employer & Industry UsagePharmaceutical companies, biotech firms, research organizationsHospitals, research institutions, pharmaceutical companies
Common Search & ComparisonYesYes

Entry Level Clinical Trials roles typically involve assisting with clinical trial activities under supervision, focusing on data collection and patient coordination. Clinical Research Coordinators have more responsibility in managing entire trial processes, ensuring compliance, and coordinating between teams. While both roles work in clinical research environments, Coordinators usually require more experience and education, making Entry Level Clinical Trials suitable for those starting in the industry.

How to get into working on entry level clinical trials?

To work in entry-level clinical trials, candidates typically need a high school diploma or equivalent, with some roles requiring a post-secondary certificate or degree in health sciences. Gaining relevant skills such as understanding Good Clinical Practice (GCP) guidelines, basic medical knowledge, and familiarity with clinical trial protocols can improve chances; certifications like Certified Clinical Research Associate (CCRA) are also beneficial. Entry-level positions often involve tasks like patient screening, data entry, and assisting with trial procedures, and may require flexibility for shift work or on-site presence.

What are the most commonly searched types of Clinical Trials jobs in Michigan?

The most popular types of Clinical Trials jobs in Michigan are:

What are popular job titles related to Entry Level Clinical Trials jobs in Michigan?

For Entry Level Clinical Trials jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Trials jobs in Michigan look for?

The top searched job categories for Entry Level Clinical Trials jobs in Michigan are:

Entry Level Clinical Trials jobs near you
Infographic showing various Entry Level Clinical Trials job openings in Michigan as of August 2026, with employment types broken down into 3% As Needed, 68% Full Time, 18% Part Time, 2% Temporary, 8% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $113,337 per year, or $54.5 per hour.

International Medical Graduate (IMG) - Clinical Research

Revival Research Institute, LLC

Southfield, MI • On-site

Full-time

Re-posted 29 days ago

Job description

Unique opportunity to make an Impact in the healthcare industry… 

Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.  

As Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.  

We are seeking International Medical Graduates with a minimum of 1 year of research experience. Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.  

New Staff should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Some responsibilities will include coordinating and managing multiple studies. They are also responsible for assisting the Principal Investigators and other clinical staff, with any study related tasks as follows but not limited to: 

  1. Research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable. 

  2. Document study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents. 

  3. Maintain organization of all trial related documents and correspondence. Implement quality control and assurance methods. 

  4. Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting. 

  5. Maintain professional and technical knowledge of Clinical trials and Standards of Care. 

  6. Protect patient confidentiality. 

Preferred Qualifications 

  1. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg

  2. Radiology experience is preferred. Phlebotomy skills are also preferred.  

  3. Additional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices. 

JOIN US & GROW YOUR KNOWLEDGE & EXPERIENCE!!! 

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